DUX4 expression in FSHD muscle cells: how could such a rare protein cause a myopathy?

Facioscapulohumeral muscular dystrophy (FSHD) is one of the most frequent hereditary muscle disorders. It is linked to contractions of the D4Z4 repeat array in 4q35. We have characterized the double homeobox 4 (DUX4) gene in D4Z4 and its mRNA transcribed from the distal D4Z4 unit to a polyadenylatio...

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Detalles Bibliográficos
Autores principales: Tassin, Alexandra, Laoudj-Chenivesse, Dalila, Vanderplanck, Céline, Barro, Marietta, Charron, Sébastien, Ansseau, Eugénie, Chen, Yi-Wen, Mercier, Jacques, Coppée, Frédérique, Belayew, Alexandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3823138/
https://www.ncbi.nlm.nih.gov/pubmed/23206257
http://dx.doi.org/10.1111/j.1582-4934.2012.01647.x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3823138/
https://www.ncbi.nlm.nih.gov/pubmed/23206257
http://dx.doi.org/10.1111/j.1582-4934.2012.01647.x

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